C1q/Tumor Necrosis Factor–Related Protein-9, a Novel Adipocyte-Derived Cytokine, Attenuates Adverse Remodeling in the Ischemic Mouse Heart via Protein Kinase A Activation

BACKGROUND—C1q/tumor necrosis factor–related protein-9 (CTRP9) is a newly identified adiponectin paralog with established metabolic regulatory properties. However, the role of CTRP9 in postmyocardial infarction remodeling remains completely unknown. This study determined whether CTRP9 may regulate c...

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Veröffentlicht in:Circulation (New York, N.Y.) N.Y.), 2013-09, Vol.128 (26_suppl_1 Suppl 1), p.S113-S120
Hauptverfasser: Sun, Yang, Yi, Wei, Yuan, Yuexing, Lau, Wayne Bond, Yi, Dinghua, Wang, Xiaoliang, Wang, Yajing, Su, Hui, Wang, Xiaoming, Gao, Erhe, Koch, Walter J., Ma, Xin-Liang
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Sprache:eng
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Zusammenfassung:BACKGROUND—C1q/tumor necrosis factor–related protein-9 (CTRP9) is a newly identified adiponectin paralog with established metabolic regulatory properties. However, the role of CTRP9 in postmyocardial infarction remodeling remains completely unknown. This study determined whether CTRP9 may regulate cardiac remodeling after acute myocardial infarction (AMI) and elucidated the underlying mechanisms. METHODS AND RESULTS—Male adult mice were subject to AMI by left anterior descending coronary artery ligation or sham surgery and treated with saline (vehicle) or globular CTRP9 via peritoneal implant osmotic pumps for 6 weeks. H9C2 cardiac cell lines were used in vitro for determining underlying mechanisms. Adipocyte CTRP9 expression and plasma CTRP9 levels were both significantly reduced after AMI. Compared with vehicle, CTRP9 treatment improved animal survival rate (P
ISSN:0009-7322
1524-4539
DOI:10.1161/CIRCULATIONAHA.112.000010